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Resolving the classification rates and molecular architecture of early-onset chronic kidney disease with NephVar

2026-07-23

Abstract excerpt

The genetic architecture of early-onset chronic kidney disease (CKD) is caused by more than 200 monogenic genes, where their common diagnostic classes include congenital anomalies of the kidney and urinary tract, steroid-resistant nephrotic syndrome, nephronophthisis-related ciliopathies, chronic glomerulonephritis, and urinary stone disease. While advancements in whole-exome and whole-genome sequencing have enabl...

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Literature Corpus work
c0be281b-01c6-51c4-90e5-de83fa340b56
DOI
10.64898/2026.07.22.26358680
Open publication

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Resolving the classification rates and molecular architecture of early-onset chronic kidney disease with NephVarDOI 10.64898/2026.07.22.26358680
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